Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.
- NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_assertion description "[The pleomorphic features exhibited by LRRK2 mutation carriers and the central role of Lrrk2 protein in the proper functioning of central nervous system suggest that mutations in this protein might be involved in multiple cellular processes leading to other neurodegenerative disorders than PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.
- NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_assertion evidence source_evidence_literature NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.
- NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_assertion SIO_000772 19822953 NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.
- NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_assertion wasDerivedFrom befree-20150227 NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.
- NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_assertion wasGeneratedBy ECO_0000203 NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP967386.RAXrS9njIXFyi2CmvPdLMJIOYDTokdmJs6KZXl25qCgMA130_provenance.